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Benzil acetylation

Thiirenes are photochemically converted to thioketenes or to alkynylthiols (Scheme 22) (80PAC1623). 2-Acetyl-3-methylthiirene rearranges on irradiation at 310 nm to a mixture of acetylmethylthioketene and thioacetylmethylketene, identified by their IR spectra (80NJC703). 2,3-Diphenylthiirene 1-oxide at 130 °C is believed to be isomerized to monothiobenzil which is air-oxidized to benzil (Scheme 23) (79JA390). [Pg.143]

Amino-5-hydrazinopyrazole dihydrochloride 300 is a good source for the synthesis of this type of heterocyclic compound [78JCS(P1)885] and it was prepared by reaction of malononitrile with two equivalents of hydrazine. Reaction of 300 with ethyl pyruvate afforded 301. Unstable hydra-zone 302 formed when 300 was boiled with diacetyl rapidly cyclized to 303. Reaction of 300 with benzil gave 304 directly, which gave an acetyl derivative and resisted reductive deamination. On the other hand, a polymer was isolated from the reaction of 300 with glyoxal (Scheme 65). [Pg.77]

Figure 6.10. Rate constants for quenching of sensitizers by cis- and trans-stilbenes (open and filled circles, respectively). Sensitizers are as follows (1) tri-phenylene, (2) thioxanthone, (3) phenanthrene, (4) 2-acetonaphthone, (3) 1-naphthyl phenyl ketone, (6) crysene, (7) fluorenone, (8) 1,2,5,6-dibenzanthracene, (9) benzil, (10) 1,2,3,4-dibenzanthracene, (11) pyrene, (12) 1,2-benzanthracene, (13) benzanthrone, (14) 3-acetyl pyrene, (15) acridine, (16) 9,10-dimethyl-l,2-benzanthracene, (17) anthracene, (18) 3,4-benzpyrene.<57> Reprinted by permission of the American Chemical Society. Figure 6.10. Rate constants for quenching of sensitizers by cis- and trans-stilbenes (open and filled circles, respectively). Sensitizers are as follows (1) tri-phenylene, (2) thioxanthone, (3) phenanthrene, (4) 2-acetonaphthone, (3) 1-naphthyl phenyl ketone, (6) crysene, (7) fluorenone, (8) 1,2,5,6-dibenzanthracene, (9) benzil, (10) 1,2,3,4-dibenzanthracene, (11) pyrene, (12) 1,2-benzanthracene, (13) benzanthrone, (14) 3-acetyl pyrene, (15) acridine, (16) 9,10-dimethyl-l,2-benzanthracene, (17) anthracene, (18) 3,4-benzpyrene.<57> Reprinted by permission of the American Chemical Society.
Benzidine, N,N -diethyl-, 36, 21 Benzidine dihydrochloride, 36, 22 Bcnzil, 34, 42 Benzil dihydrazone, 34, 42 Benzilic acid, 33, 37 2-Benzimidazolethiol, 30, 56 l,2-Benzo-3,4-dihydrocarbazole, 30, 91 Benzofuran, 3-methyl, 33, 43 Benzofurazan oxide, 31,14, 15 37,1 Benzoguanamine, 33,13 Benzoic acid, 32, 94 37, 21 Benzoic acid, -acetyl-, methyl ester, 32, 81... [Pg.45]

Many oxidizing agents have been used, especially copper sulfate and other cupric salts. Potassium dichromate in acetic acid and manganese dioxide are good oxidants for benzil bis(phenylhydrazone). Nitrous acid has been used for the osazones of acetylated sugars and for phenylglyoxal bis(phenylhydrazone). ... [Pg.59]


See other pages where Benzil acetylation is mentioned: [Pg.82]    [Pg.779]    [Pg.82]    [Pg.779]    [Pg.52]    [Pg.205]    [Pg.25]    [Pg.85]    [Pg.82]    [Pg.779]    [Pg.647]    [Pg.454]    [Pg.647]    [Pg.94]    [Pg.210]    [Pg.577]    [Pg.647]    [Pg.480]    [Pg.481]    [Pg.25]    [Pg.41]    [Pg.626]    [Pg.1086]    [Pg.82]    [Pg.779]    [Pg.420]    [Pg.97]    [Pg.1538]    [Pg.82]    [Pg.779]    [Pg.41]   
See also in sourсe #XX -- [ Pg.420 ]




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